Form 483

Surgical Direct, Inc. Form 483, 2018-08-03

FDA issued a Form 483 to Surgical Direct, Inc. on 2018-08-03 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Surgical Direct, Inc. · Orange City, United States · Issued August 3, 2018

Overview

  • 8 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

3 Aug 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Richard K Vogel

3 Aug 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Richard K Vogel

3 Aug 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Richard K Vogel

3 Aug 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Richard K Vogel

3 Aug 2018
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Richard K Vogel

Inspected site

SDSurgical Direct, Inc.Orange City, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50Cited across public-safe Form 483 observations2x
21 CFR 820.80(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 8 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere